64
1
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7775 |
A2764 dihydrochloride
|
Potassium Channel | Membrane transporter/Ion channel |
A2764 dihydrochloride 是高选择性的TRESK (K2P18.1)抑制剂,对 TREK-1 和 TALK-1 有抑制作用。它相比基底 mTRESK 电流,对激活渠道更敏感 (IC50= 6.8 μM)。它可导致细胞去极化,增加细胞的兴奋性,在探索 TRESK 通道在偏头痛和痛觉中的作用中具有研究的价值。 | |||
T1092 |
Zolmitriptan
佐米曲普坦,311C90,BW-311C90 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Zolmitriptan (311C90) 是一种5-HT1B/1D 受体部分激动剂,可用于偏头痛的研究,对 5-HT1B、5-HT1D、5-HT1F 受体的Ki 分别为 5.01、0.63 和 63.09 nM。 | |||
T8682 |
Vazegepant hydrochloride
Vazegepant HCl |
CGRP Receptor | GPCR/G Protein; Neuroscience |
Vazegepant hydrochloride (Vazegepant HCl) 是一种用于偏头痛的鼻用 gepant,是一种高度亲和性CGRP 受体拮抗剂 (hCGRPKi=0.023 nM)。它可能有助于有效管理 COVID-19 相关肺部炎症。 | |||
T0203 |
Sumatriptan succinate
舒马普坦琥珀酸盐,GR 43175,琥珀酸舒马曲坦 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Sumatriptan succinate (GR 43175) 是一种5-HT1受体激动剂,可作用于偏头疼的急性治疗。 | |||
T1602 |
Valproic acid sodium salt
丙戊酸钠,Sodium Valproate |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic acid sodium salt (Sodium Valproate) 是一种HDAC 抑制剂,可抑制HDAC1的活性,诱导HDAC2的降解。它激活Notch1信号并抑制小细胞肺癌细胞的增殖。它可研究癫痫、偏头痛和双相情感障碍等。 | |||
T11326 |
Frovatriptan succinate hydrate
Frovelan,夫罗曲坦琥珀酸盐水合物 ,Frova |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Frovatriptan succinate hydrate (Frova) 是一种有效、高亲和力、选择性和口服活性的 5-HT1B、HT1D 受体激动剂和中等有效的 5-HT7 受体激动剂,pKi 值分别为 8.6、8.4 和 6.7。它可有效治疗各种偏头痛,包括恶心、呕吐、畏光和畏声等相关症状。 | |||
T6474 |
Divalproex Sodium
Valproate semisodium,Epival,双丙戊酸钠 |
HDAC | Chromatin/Epigenetic; DNA Damage/DNA Repair |
Divalproex Sodium (Valproate semisodium) 结合并抑制 γ-氨基丁酸 (GABA) 转氨酶,其抗惊厥活性可通过增加 GABA 脑浓度和抑制分解 GABA 或阻止 GABA 再摄取到神经胶质和神经末梢的酶来发挥。它也是一种 HDAC 抑制剂。由丙戊酸钠和丙戊酸组成,具有抗惊厥和抗癫痫活性。 Divalproex 还可以通过抑制电压敏感的钠通道来抑制重复的神经元放电。 | |||
T5479 |
AMG 333
AMG-333 |
TRP/TRPV Channel | Membrane transporter/Ion channel |
AMG 333 是有效的TRPM8高选择性拮抗剂,IC50为13 nM。 | |||
T8666 |
Naratriptan
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Naratriptan 是一种5-HT1受体选择性激动剂,可作用于偏头疼。 | |||
T69096 |
Femoxetine hydrochloride
|
5-HT Receptor | GPCR/G Protein; Neuroscience |
Femoxetine hydrochloride 是一种选择性5-羟色胺再摄取抑制剂,可用于研究偏头痛,抑郁和饮食失调。 | |||
T27932 |
LY-2300559
LY2300559 |
GluR | Neuroscience |
LY-2300559 是代谢型谷氨酸受体 2 (mGluR2) 的激动剂,可用于偏头痛治疗的研究。 | |||
T68145 |
Stacofylline
|
||
Stacofylline 是一种黄嘌呤衍生物,可用于治疗偏头疼。 | |||
T31208 |
Dasolampanel
NGX-426,NGX 426,NGX426 |
GluR; iGluR | Membrane transporter/Ion channel; Neuroscience |
Dasolampanel (NGX-426) 是一种可口服的离子型谷氨酸受体 AMPA 和 Kainate 受体拮抗剂,可用于研究慢性疼痛疾病,包括神经性疼痛和偏头痛。 | |||
T68067L |
Etilefrine pivalate HCl
Etilefrine pivalate HCl(100696-30-8 Free base) |
||
Etilefrine pivalate HCl 是一种具有口服活性的化合物,可用于治疗偏头痛。 | |||
T8993L |
BGC-20-1531 hydrochloride(1186532-61-5 free base)
BGC-20-1531 hydrochloride,GTPL3380 hydrochloride,AP-1531 hydrochloride |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
BGC-20-1531 hydrochloride(1186532-61-5 free base) (GTPL3380 hydrochloride) 是一种 EP4 拮抗剂,用于治疗急性偏头痛。 | |||
T17194 |
Ubrogepant
MK-1602 |
CGRP Receptor | GPCR/G Protein; Neuroscience |
Ubrogepant (MK-1602) 是新型的、口服有效的降钙素基因相关肽受体拮抗剂。Ubrogepant 有潜力用于急性偏头痛的相关研究。 | |||
T6571 |
Lomerizine dihydrochloride
Terranas,盐酸洛美利嗪,Lomerizine 2HCl,Lomerizine hydrochloride,KB-2796 |
Calcium Channel | Membrane transporter/Ion channel; Metabolism |
Lomerizine dihydrochloride (KB-2796) 是双重 L 和 T 型电压门控钙通道拮抗剂。 | |||
T76874 |
Erenumab
AMG-334 |
CGRP Receptor | GPCR/G Protein; Neuroscience |
Erenumab是一种全人单克隆抗体,作用于抑制降钙素基因相关肽(CGRP)受体,用于预防发作性偏头痛。 | |||
T77513 |
2-Chlorophenylboronic acid
|
FAAH | Metabolism; Neuroscience |
2-Chlorophenylboronic acid 是一种单卤代苯硼酸,是一种重要的医药中间体,在新药合成中应用广泛。2-Chlorophenylboronic acid 对脂肪酸酰胺酶有抑制作用,Ki 值为0.01-1 µM,可用于研究抑郁症、青光眼、神经性疼痛、焦虑、偏头痛、I 型糖尿病和胃炎等疾病。 | |||
T2317 |
Almotriptan Malate
LAS 31416,PNU180638,马来酸阿莫曲坦 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Almotriptan Malate (PNU180638) 是一种选择性 5-HT1B/1D 受体激动剂,用于治疗成人偏头痛发作。 | |||
T17285 |
Zatosetron maleate
LY 277359 maleate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Zatosetron maleate(LY 277359 maleate) 是一种具有有效性和选择性的血清素 5HT3 受体拮抗剂,可用于研究急性偏头痛。 | |||
T25615 |
Lanepitant
LY303870,LY-303870,LY 303870 |
Others | Others |
Lanepitant (LY303870) 是一种非肽类神经激肽-1(NK-1)拮抗剂,具有镇痛活性,可抑制神经源性硬脑膜炎症,可用于预防偏头痛。 | |||
T1512 |
Rizatriptan benzoate
苯甲酸利扎曲坦,MK-462 Benzoate |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Rizatriptan benzoate (MK-462 Benzoate) 是 5-HT1激动剂,通过选择性结合并激活血清素 (5-HT) 1B 受体和 5-HT 1D 受体,从而缓解偏头痛。 | |||
T14384 |
AZD8797
KAN-0440567,KAND567 |
CXCR | Autophagy; GPCR/G Protein; Immunology/Inflammation |
AZD8797 (KAND567) 是一种可口服且具有选择性和有效性的人 CX3CR1 变构拮抗剂,对 CX3CR1 和 CXCR2 具有抑制作用,对SARS-CoV-2诱导的神经元损伤有潜在的保护作用,可防止癫痫发作后偏头痛模型大鼠痛觉过敏和小胶质细胞活化的恶化。 | |||
T34609 |
Selurampanel
BGG-492,BGG 492,BGG492 |
iGluR | Membrane transporter/Ion channel; Neuroscience |
Selurampanel (BGG492) 是一种具有口服活性和选择性的竞争性 AMPA 谷氨酸受体拮抗剂,是一种喹唑啉二酮磺酰胺。Selurampanel 可用于研究癫痫、偏头痛和耳鸣。 | |||
T6602 |
Naratriptan hydrochloride
Naratriptan HCl,Amerge,Naramig,盐酸那拉曲坦,GR-85548A hydrochloride |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Naratriptan hydrochloride (GR-85548A hydrochloride) 是一种5-HT1受体激动剂,有抗偏头疼特性。它还可以通过刺激三叉神经系统感觉神经末梢上的 5-HT1D/1B 受体来发挥其作用,从而减少促炎神经肽的释放。 | |||
T4008 |
Metergoline
甲麦角林,Methergoline,Liserdol |
Dopamine Receptor; 5-HT Receptor; Sodium Channel | GPCR/G Protein; Membrane transporter/Ion channel; Neuroscience |
Metergoline (Methergoline) 是多巴胺激动剂和血清素拮抗剂。它是 h5-HT7受体的高亲和力配体,Ki 为 16 nM。它还是可逆神经 Na+通道抑制剂,用于研究季节性情绪障碍、催乳激素调节。 | |||
T21231 |
Almotriptan
阿莫曲坦,LAS 31416,阿莫曲普坦 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Almotriptan (LAS 31416) 是一种用于研究偏头痛的5-HT1B/1D 受体激动剂。 | |||
T0806 |
Flunarizine dihydrochloride
Flunarizine 2HCl,KW-3149,R14950,盐酸氟桂利嗪 |
Calcium Channel; Dopamine Receptor; Sodium Channel | GPCR/G Protein; Membrane transporter/Ion channel; Metabolism; Neuroscience |
Flunarizine dihydrochloride (R14950) 是 Na+/Ca2+(T 型) 通道双重阻滞剂。它也是 D2多巴胺受体拮抗剂。它具有用于扩张外周血管和预防偏头痛的潜力。 | |||
T0784 |
Tolfenamic Acid
托芬那酸,GEA 6414,托灭酸,Tolfedine |
COX | Immunology/Inflammation; Neuroscience |
Tolfenamic Acid (GEA 6414) 是一种非甾体抗炎剂和抗癌剂,可用于治疗偏头痛的症状。它能选择性地抑制COX-2的活性,在 LPS 诱导的犬 DH82 单核细胞/巨噬细胞中,对COX-2的IC50值为 13.49 μM(3.53 μg/mL)。 | |||
T1442 |
Pizotifen
Pizotyline,BC-105,苯噻啶 |
5-HT Receptor | GPCR/G Protein; Neuroscience |
Pizotifen (Pizotyline) 是5-HT2受体的有效拮抗剂,并对5-HT1C 有高亲和力。它是一种强血清素和色胺拮抗剂,具有较弱的抗胆碱能、抗组胺和抗激肽作用,还具有镇静和刺激食欲的特性。 | |||
T69734 |
Org GC 94
|
||
Org GC 94 is a serotonin antagonist; anti-migraine. | |||
T27628 |
IS-159
IS 159,IS159 |
||
IS-159, a 5-HT1D agonist, is used potentially for the treatment of migraine. | |||
T39522 |
HTL22562
|
||
HTL22562 is a calcitonin gene-related peptide (CGRP) receptor antagonist for acute treatment of migraine. | |||
T26079 |
RI 61
RI-61,Pro-his-pro-phe-his-leu-phe-val-phe,RI61 |
||
RI 61 (sumatriptan succinate) is utilized in the therapy of migraine, cluster headaches, new daily persistent headache, and cyclic vomiting syndrome. | |||
T27915 |
LY 302148
LY-302148,LY302148 |
||
LY 302148 , a 5-HT1F receptor agonist, inhibits neurogenic dural inflammation in guinea pigs. It has potential for migraine therapeutics. | |||
T70997 |
Fonazine mesylate
|
||
Fonazine mesylate is a phenothiazine drug used for the treatment of migraine. It is a serotonin antagonist and histamine antagonist. | |||
T38734 |
Vazegepant
Zavegepant,BHV-3500 |
||
Vazegepant is an intranasal CGRP receptor antagonist utilized for conducting acute migraine research. | |||
T21407 |
Frovatriptan Succinate
Frovatriptan succinate hydrate,NCGC00183880-01,Frovatriptan Succinate monohydrate,KB-295988 |
||
Frovatriptan Succinate is a synthetic triptan with 5-HT1B/1D receptors agonist activity. It is indicated for the acute treatment of migraine. | |||
T8993 |
BGC201531
AP-1531,GTPL3380,BGC-20-1531 |
Prostaglandin Receptor | GPCR/G Protein; Immunology/Inflammation |
BGC201531 (AP-1531) 是一种 EP4 拮抗剂,用于治疗急性偏头痛。 | |||
T26598 | Alniditan dihydrochloride | ||
Alniditan dihydrochloride is a potent 5-HT1D agonist and migraine-abortive agent. | |||
T26781 |
BF-1
BF1 |
||
BF-1 is a 5-Hydroxytryptamine receptor 2B antagonist. BF-1 was tested as potential migraine prophylactic drug by blocking BW723C86 (5-((thiophen-2-yl)methoxy)-α-methyltryptamine) or meta-chlorophenylpiperazine (mCPP) induced neurogenic dural plasma protei | |||
T30229 |
Avitriptan Fumarate
BMS 180048,BMS180048,BMS-180048,UNII-2G25KE3954 |
||
Amitriptan fumarate is serotonin 5HT-1B/1D receptor agonist with anti-migraine activity. | |||
T34832 |
Tezampanel hydrate
LY293558,NGX 424,NGX424,LY-293558,NGX-424,LY 293558 |
||
Tezampanel is used for the treatment of migraine, neuropathic pain. | |||
T25617 |
Lanepitant HCl trihydrate
Lanepitant dihydrochloride trihydrate |
||
Lanepitant HCl trihydrate is an effective non-peptide neurokinin-1 receptor antagonist, suppresses neurogenic dural inflammation, and may have a role in migraine therapy. | |||
T32105 |
Cipepofol
HSK3486,HSK 3486,HSK-3486 |
||
HSK3486 is similar to propofol and is a general anesthetic, which may have therapeutic potential in insomnia, migraine, anxiety, analgesia, and other aspects. | |||
T31844 |
Fonazine
Dimethodin,Banistyl,Dimetiotazine,Dimetotiazine,Dimethothiazine |
||
Forazine (dimethiazide) is a phenothiazine drug used in the treatment of migraine and is a serotonin antagonist and a histamine antagonist. | |||
T69407 | Fonazine hydrochloride | ||
Fonazine hydrochloride is a phenothiazine drug used for the treatment of migraine. It is a serotonin antagonist and histamine antagonist. | |||
T21392 |
Flunarizine
Flunarizinum,Flunarizin,Sibelium,Flunarizina,R-14950 |
||
Flunarizine is a non-selective calcium entry blocker and a histamine H1 receptor blocker. It is effective in the prophylaxis of migraine, occlusive peripheral vascular disease, vertigo of central and peripheral origin, and as an adjuvant in the therapy of | |||
T70410 | Cam 2445 | ||
Cam 2445 is a nonpeptide, alpha-methyltryptophan derivative; an NK1 neurokinin receptor antagonist that is a potentially useful treatment for arthritis, asthma, migraine, anxiety, psychosis, and emesis. |
Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T7064 |
Valproic Acid
Sodium valproate,2-Propylpentanoic Acid,丙戊酸,VPA,Depakine,2-Propylvaleric Acid |
Mitophagy; Gamma-secretase; HIV Protease; GABA Receptor; Sodium Channel; HDAC; Autophagy | Autophagy; Chromatin/Epigenetic; DNA Damage/DNA Repair; Membrane transporter/Ion channel; Microbiology/Virology; Neuroscience; Proteases/Proteasome; Stem Cells |
Valproic Acid (2-Propylpentanoic Acid) 是一种 HDAC 抑制剂,可抑制 HDAC1 活性,诱导 HDAC2 降解,具有口服活性。Valproic Acid 可以用于癫痫和躁郁症的研究。 |